Ampicillin Powder For Solution For Injection 10G Drug Medication Dosage Information
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Ampicillin: Powder for solution for injection (10g)

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What is this Medicine?

AMPICILLIN (am pi SILL in) is a penicillin antibiotic. It is used to treat certain kinds of bacterial infections. It will not work for colds, flu, or other viral infections.

In-Depth Information
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Ampicillin 10g Bulk Powder for Injection

NDC: 000690026
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Typhoid Fever, Meningitis, Salmonellosis, Upper Respiratory Tract Infections, Septicemia, Vancomycin-resistant Enterococci (VRE), Cystitis, Endocarditis, Gastroenteritis, Cellulitis, Pyelonephritis, Enterocolitis, Skin And Skin Structure Infections, Shigellosis, Urinary Tract Infection (UTI), Lower Respiratory Tract Infections, Community-acquired Pneumonia

Sometimes used for but not FDA approved for the following conditions:
Leptospirosis, Endocarditis Prophylaxis, Bacterial Infection Prophylaxis

Storage Information
Store between 68 to 77 degrees F, excursions permitted 59 to 86 degrees F
Ampicillin 10g Bulk Powder for Injection

Reported Side Effects for Ampicillin 10g Bulk Powder for Injection

Skin Rash Incidence:
<5.0%*
Severity: MILD
Onset: EARLY
Rash With Pustules Incidence:
<5.0%*
Severity: MILD
Onset: EARLY
Hives Incidence:
<5.0%*
Severity: MILD
Onset: RAPID
Serum Sickness Incidence:
<5.0%*
Severity: SEVERE
Onset: DELAYED
Itching Incidence:
<5.0%*
Severity: MILD
Onset: RAPID
Exfoliative Dermatitis Incidence:
<5.0%*
Severity: SEVERE
Onset: DELAYED
Erythema Multiforme Incidence:
<5.0%*
Severity: SEVERE
Onset: DELAYED
Upset Stomach Incidence:
2.0-5.0%*
Severity: MILD
Onset: EARLY
Tongue Discoloration Incidence:
2.0-5.0%*
Severity: MILD
Onset: DELAYED
Loose Stools Incidence:
2.0-5.0%*
Severity: MILD
Onset: EARLY
Inflamed Intestine Incidence:
2.0-5.0%*
Severity: SEVERE
Onset: DELAYED
Inflamed Tongue Incidence:
2.0-5.0%*
Severity: MODERATE
Onset: EARLY
Vomiting Incidence:
2.0-5.0%*
Severity: MILD
Onset: EARLY
Mouth Ulcers Incidence:
2.0-5.0%*
Severity: MODERATE
Onset: DELAYED
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
FIRST Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

SECOND Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

THIRD Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

Lactation

Compatible - This drug is generally safe to take by nursing mothers.


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